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FDA 510(k) Applications Submitted by HDI, Inc.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K222741
09/09/2022
DENU Light Body(Regular, Fast), DENU Heavy Body(Regular, Fast), DENU Putty Set(Regular, Fast)
HDI, Inc.
K213339
10/07/2021
DENU Composite Resin, DENU Flow Resin
HDI, Inc.
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